FDA Inspection 1039547 - Hospira, Inc. - February 02, 2018

FDA Inspection 1039547 for Hospira, Inc. on February 02, 2018. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1039547 for Hospira, Inc. on February 02, 2018. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 211.100(b)

21 CFR 211.160(b)(4)

21 CFR 211.68(a)

21 CFR 820.100(b)

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Record Information

Company

Hospira, Inc.

Inspection Date

February 2, 2018

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: cda69c71-b01f-446f-b536-c0289c163dae

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